Drug General Information (ID: DDIOR6NWYQ)
  Drug Name Vincristine Drug Info Guselkumab Drug Info
  Drug Type Small molecule Monoclonal antibody
  Therapeutic Class Antineoplastics Interleukin Inhibitors

 Mechanism of Vincristine-Guselkumab Interaction (Severity Level: Moderate)
     Additive immunosuppressive effects Click to Show/Hide Mechanism Graph
Could Not Find 2D Structure
      Drug Name Vincristine Guselkumab
      Mechanism 1 Immunosuppressive effects Immunosuppressive effects
      Key Mechanism Factor 1
Factor Name Immunosuppressive effects
Factor Description Immunosuppression is when your immune system is not functioning as it should. The immune system is made up of cells, tissues and organs that help the body fight off infections. If the immune system is suppressed, an infection that your body was able to control may become serious or even fatal.
      Mechanism Description
  • Additive immunosuppressive effects by the combination of Vincristine and Guselkumab 
     Additive myelosuppressive effects Click to Show/Hide Mechanism Graph
Could Not Find 2D Structure
      Drug Name Vincristine Guselkumab
      Mechanism 2 Myelosuppressive effects Myelosuppressive effects
      Key Mechanism Factor 2
Factor Name Myelosuppressive effects
Factor Description Myelosuppression, also known as bone marrow suppression, is a decrease in bone marrow activity that leads to a decrease in the production of blood cells. Some blood cell disorders include: erythrocytopenia (anemia), leukopenia (neutropenia), and thrombocytopenia (thrombocytopenia).
      Mechanism Description
  • Additive myelosuppressive effects by the combination of Vincristine and Guselkumab 

Recommended Action
      Management Concomitant use of interleukin blockers with other immuno- or myelosuppressive agents should be avoided if possible. Caution is advised when interleukin inhibitors are prescribed to patients receiving concomitant drugs that are CYP450 substrates, particularly those with narrow therapeutic ranges such as immunosuppressants or antineoplastic agents. Clinical and/or laboratory monitoring should be considered following the initiation or withdrawal of interleukin inhibitor therapy, and the dosage(s) of these drugs adjusted accordingly. Clinicians should note that the effects of interleukin inhibitors on CYP450 activities may persist for several weeks after stopping therapy.

References
1 Cerner Multum, Inc. "UK Summary of Product Characteristics.".
2 Product Information. Actemra (tocilizumab). Genentech, South San Francisco, CA.
3 Product Information. Amevive (alefacept). Biogen, Cambridge, MA.
4 Product Information. Arcalyst (rilonacept). Regeneron Pharmaceuticals Inc, Tarrytown, NY.
5 Product Information. Cosentyx (secukinumab). Novartis Pharmaceuticals, East Hanover, NJ.
6 Product Information. Ilaris (canakinumab). Novartis Pharmaceuticals, East Hanover, NJ.
7 Product Information. Stelara (ustekinumab). Centocor Inc, Malvern, PA.
8 Product Information. Sylvant (siltuximab). Janssen Biotech, Inc., Horsham, PA, PA.
9 Product Information. Taltz Autoinjector (ixekizumab). Eli Lilly and Company, Indianapolis, IN.